Polar nuclear localization of H1T2, a histone H1 variant, required for spermatid elongation and DNA condensation during spermiogenesisp75 neurotrophin receptor is a clock gene that regulates oscillatory components of circadian and metabolic networksThe nuclear import of TAF10 is regulated by one of its three histone fold domain-containing interaction partnersCommon pathways in circadian and cell cycle clocks: light-dependent activation of Fos/AP-1 in zebrafish controls CRY-1a and WEE-1Mitotic phosphorylation of histone H3: spatio-temporal regulation by mammalian Aurora kinasesThyroid-stimulating hormone (TSH)-directed induction of the CREM gene in the thyroid gland participates in the long-term desensitization of the TSH receptorThe NAD+-dependent deacetylase SIRT1 modulates CLOCK-mediated chromatin remodeling and circadian controlRegulation of metabolism: the circadian clock dictates the timeThe circadian clock transcriptional complex: metabolic feedback intersects with epigenetic controlROS stress resets circadian clocks to coordinate pro-survival signalsNovel insights into the downstream pathways and targets controlled by transcription factors CREM in the testisCK2alpha phosphorylates BMAL1 to regulate the mammalian clock.The intracellular localisation of TAF7L, a paralogue of transcription factor TFIID subunit TAF7, is developmentally regulated during male germ-cell differentiationDistinct functions of TBP and TLF/TRF2 during spermatogenesis: requirement of TLF for heterochromatic chromocenter formation in haploid round spermatidsNovel regulation of cardiac force-frequency relation by CREM (cAMP response element modulator)Temporal association of protamine 1 with the inner nuclear membrane protein lamin B receptor during spermiogenesisCircadian regulator CLOCK is a histone acetyltransferaseSpermiogenesis deficiency and germ-cell apoptosis in CREM-mutant miceImpact of Sleep and Circadian Disruption on Energy Balance and Diabetes: A Summary of Workshop DiscussionsKetamine influences CLOCK:BMAL1 function leading to altered circadian gene expressionTIPT, a male germ cell-specific partner of TRF2, is chromatin-associated and interacts with HP1Interplay of PIWI/Argonaute protein MIWI and kinesin KIF17b in chromatoid bodies of male germ cellsProtein phosphatase PHLPP1 controls the light-induced resetting of the circadian clockSignaling mediated by the dopamine D2 receptor potentiates circadian regulation by CLOCK:BMAL1Photoinducible and rhythmic ICER-CREM immunoreactivity in the rat suprachiasmatic nucleusChanges in intranuclear chromatin architecture induce bipolar nuclear localization of histone variant H1T2 in male haploid spermatidsPER2 controls lipid metabolism by direct regulation of PPARγInducible cAMP early repressor regulates the Period 1 gene of the hepatic and adrenal clocksProteolytic cleavage of ALF into alpha- and beta-subunits that form homologous and heterologous complexes with somatic TFIIA and TRF2 in male germ cellsImpaired light masking in dopamine D2 receptor-null miceProduction of fertile offspring from genetically infertile male miceThe RelB subunit of NFκB acts as a negative regulator of circadian gene expressionThe histone methyltransferase MLL1 permits the oscillation of circadian gene expressionMouse Period1 (mPER1) acts as a circadian adaptor to entrain the oscillator to environmental light/dark cycles by regulating mPER2 proteinTranscriptional control in male germ cells: general factor TFIIA participates in CREM-dependent gene activation.Functional analysis of transcription factors CREB and CREM.CREM gene: use of alternative DNA-binding domains generates multiple antagonists of cAMP-induced transcription.Regulation of BMAL1 protein stability and circadian function by GSK3beta-mediated phosphorylation.A small C-terminal sequence of Aurora B is responsible for localization and functionCell-specific occupancy of an extended repertoire of CREM and CREB binding loci in male germ cells
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